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Gene TP53
Variant R175X
Impact List missense
Protein Effect unknown
Gene Variant Descriptions TP53 R175X indicates a hotspot mutation resulting in an amino acid change at codon 175 of the Tp53 protein, which often results in a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon5 TP53 R175X

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Transcript NM_000546.6
gDNA chr17:g.7675087_7675089
cDNA c.523_525
Protein p.R175
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001126114.3 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126112 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_000546 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126114 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126113 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.7675087_7675089 c.523_525 p.R175 RefSeq GRCh38/hg38

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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries